Rs104894146

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Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs104894146(G;G)
Make rs104894146(G;T)
ReferenceGRCh38 38.1/141
Chromosome10
Position102837084
GeneCYP17A1
is asnp
is mentioned by
dbSNPrs104894146
Exacrs104894146
PheGenIrs104894146
nextbiors104894146
hapmaprs104894146
1000 genomesrs104894146
hgdprs104894146
ensemblrs104894146
gopubmedrs104894146
geneviewrs104894146
scholarrs104894146
googlers104894146
pharmgkbrs104894146
gwascentralrs104894146
openSNPrs104894146
23andMers104894146
23andMe allrs104894146
SNP Nexus

SNPshotrs104894146
SNPdbers104894146
MSV3drs104894146
Max Magnitude0
OMIM609300
Desc
Variant0018
Relatedalso
ClinVar
Risk rs104894146(G;G)
Alt rs104894146(G;G)
Reference rs104894146(T;T)
Significance Pathogenic
Disease Complete combined 17-alpha-hydroxylase/17
Variation info
Gene CYP17A1
CLNDBN Complete combined 17-alpha-hydroxylase/17,20-lyase deficiency
Reversed 1
HGVS NC_000010.10:g.104596841A>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000001864.1,